English
新闻公告
More
化学进展 1998, Vol. 10 Issue (03): 285- 前一篇   后一篇

• 综述与评论 •

微波促进有机化学反应研究进展

樊兴君;焦天权;谭干祖;俞贤达;尤进茂   

  1. 兰州大学化学系;中科院兰州化学物理所
  • 收稿日期:1997-08-01 修回日期:1997-11-01 出版日期:1998-09-24 发布日期:1998-09-24
  • 通讯作者: 谭干祖

Progress in Microwave-Organic Reaction Enhancement Chemistry

Fan Xingjun;You Jinmao;Tan Ganzu;Yu Xianda;Jiao Tianquan   

  1. Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences,Lanzhou 730000, China Department of Chemistry, Lanzhou U niversity, Lanzhou 730000, China"
  • Received:1997-08-01 Revised:1997-11-01 Online:1998-09-24 Published:1998-09-24
  • Contact: Tan Ganzu

微波促进有机化学反应是一个新的技术。本文介绍了近年来该技术在有机化学领域中的应用情况, 共引用文献68 篇。

Microwave organic reaction enhancement chemistry is a novelmethod. This paper focuses on the applications of microwave irradiation (MWI) in organic synthesis in recent years. 68 references are cited.

中图分类号: 

()

[1 ] Gedye R N , Smith F E, Westaway K C et al. , Tetrahedron Lett. , 1986, 27, 2791
[2 ] Cole K S, Cole R H, J. Chem. Phys. , 1941, 9, 341- 351.
[3 ] Frohlich H, Theory of Dielectrics, 2nd edit. , Oxford University Press, London, 1958.
[4 ] Gedye R N , Smith F E, Westaway K C, J. Microwave Power Electromagn. Energy , 1991, 26, 3-17.
[5 ] Baghurst D R, Mingos D M P, J. Organomet. Chem. , 1990, 384, C57- C60.
[6 ] Chen S T , Chiou S H, Wang K T , J. Chem. Soc. , Chem. Commun. , 1990, 807- 809.
[7 ] Cablewski T , Faux A F, Strauss C R, J. Org. Chem. , 1994, 59, 3408- 3412.
[8 ] Baghurst D R, Mingos D M P, J. Chem. Soc. , Dalton Trans. , 1992, 1151- 1155.
[9 ] Michael D, Mingos P, Barghurst D R, Chem. Soc. Rev. , 1991, 20, 1- 47.
[10 ] Zijlsra S, Croot T J , J. Org. Chem. , 1993, 58 (7) , 1643.
[11 ] Raner K D, Strauss C R, Trainor R W et al. , J. Org. Chem. , 1995, 60, 2456- 2460.
[12 ] Giguere R J , Herberich B, Synth. Commun. , 1991, 21 (21) , 2197- 2201.
[13 ] Gedye R N , Smith F E, Westaway K C, Can. J. Chem. , 1988, 66, 17- 26.
[14 ] Bose A K, Manhas M S, Ghosh M et al. , Heterocycles, 1990, 30, 741- 744.
[15 ] Sun W C, Guy P M , Jahngen J H et al. , J. Org. Chem. , 1988, 53, 4414- 4416.
[16 ] Lewis D A , Summers J S, Ward T C et al. , J. Polym. Sci. , Part A , Polym. Chem. , 1992, 30, 1647- 1653.
[17 ] Shibata C, Kashima T , Ohuchi K, Jpn. J. Appl. Phys. , 1996, 35, 316- 319.
[18 ] Dollington S D, Bond G, Moyes R B et al. , J. Org. Chem. , 1991, 56, 1313- 1317.
[19 ] Plazl I, Acta Chim. Slov. , 1994, 41, 437.
[20 ] Raner K D, Strauss C R, J. Org. Chem. , 1992, 57, 6231- 6234.
[21 ] Chriscopher R S, Robert W T , Aust. J. Chem. , 1995, 48, 1665- 1692.
[22 ] Giguere R J , Bray T L , Duncan S M et al. , Tetrahedron Lett. , 1986, 27, 4945- 4948.
[23 ] Illescas B, Martin N , Seoane C et al. , Tetrahedron Lett. , 1995, 36 (45) , 8307- 8310.
[24 ] Banik B K, Manhas M S, Kaluza Z et al. , Tetrahedron Lett. , 1992, 33, 3603- 3606.
[25 ] Kim J K, Kwon P S, Kwon T W et al. , Synth. Commun. , 1990, 26, 535- 542.
[26 ] DayalB, Rapole K R, Salen G et al. , Synlett, 1995, 861- 862.
[27 ] Bose A K, Manhas M S, Banik B K et al. , Res. Chem. Inter. , 1994, 20, 1- 11.
[28 ] Bose A K, Manhas M S, Ghosh M et al. , J. Org. Chem. , 1991, 56, 6968- 6970.
[29 ] Runhua D, Yuliang W , Synth. Commun. , 1994, 24, 111- 115.
[30 ] Herradon B, Morcuende A , Valverde S, Synlett, 1995, 455- 458.
[31 ] Kundu M K, Mukherjet S B, Synlett, 1994, 444.
[32 ] Yuncheng Y, Dabin G, Synth. Commun. , 1992, 22, 2117- 2119.
[33 ] Jie M S F, Kit C Y, Lipids, 1988, 23, 367.
[34 ] Loupy A , Pigeon P, J. Chem. Res. 2S. 1993, 36.
[35 ] Loupy A , Petit A , Ramdani M et al. , Can. J. Chem. , 1993, 71, 90- 95.
[36 ] Loupy A , Pigeon P, Ramdani M , Tetrahedron, 1996, 52, 6705- 6712.
[37 ] Huang Z, Zu L , Org. Prop. Proced. Int. , 1996, 28, 121- 123.
[38 ] Wang J X, Zhang M L , Xing Z L et al. , Synth. Commun. , 1996, 26, 301- 305.
[39 ] Majdoub M , Loupy A , Petit A et al. , Tetrahedron, 1996, 52, 617- 627.
[40 ] Villemin D, Labiad B, Synth. Commun. , 1990, 20, 3207- 3212.
[41 ] Villemin D, Alloum A B, Synth. Commun. , 1991, 21, 63- 68.
[42 ] Villemin D, Martin B, Garrigues B, Synth. Commun. , 1993, 23, 2251- 2257.
[43 ] Strikrishna A , Kumar P P, Tetrahedron Lett. , 1995, 36, 6313- 6316.
[44 ] Sowmya S, Balasubramanian K K, Synth. Commun. , 1994, 24, 2097- 2101.
[45 ] Gupta R, Paul S, Gupta A K et al. , Indian J. Chem. , 1994, 33B , 888- 891.
[46 ] Petit A , Loupy A , Maillard P et al. , Synth. Commun. , 1992, 22, 1137- 1142.
[47 ] 刘沫文, 胡文祥, 恽榴红, 第一届全国微波化学学术讨论会论文集, 长春, 1996, 54.
[48 ] Villemin D, Labiad B, Synth. Commun. , 1992, 22, 2043- 2052.
[49 ] Delgado F, Alvarez L , Garcia O et al. , Synth. Commun. , 1991, 21, 2137- 2141.
[50 ] Varma R S, Varma M , Chatterjee A K, J. Chem. Soc. , Perkin Trans. 1, 1993, 999- 1000.
[51 ] Beldjoudi N , Bouazizi A , Boribi D et al. , Eur. Polym. J. , 1988, 24, 49- 52.
[52 ] Imai Y, Nemoto H, J. Polymer Sci. , Part A , Polym. Chem. , 1996, 34, 701- 704.
[53 ] Gaghani J , Lee R, Wilcoxson A L , US 4 305 796A , 1981 (Chem. Abstr. , 1982, 97, 24654v).
[54 ] Morimoto H, Yoshioka H, J P 02 107 638, 1990 (Chem. Abstr. , 1990, 113, 79264x).
[55 ] SilinskiB, Kuzmycz C, Gourdenne A , Eur. Polym. J. , 1987, 23, 273- 277.
[56 ] Irie S, Asada Y, J P 54 073 841, 1979 (Chem. Abstr. , 1979, 91, 194143w ).
[57 ] Wen Y S, Miyazaki K, Horibe T , Fukuoka Shika Daigaku Gakkai Zasshi, 1987, 14 (2) , 158_ 162(Chem. Abstr. , 1988, 108, 101312g).
[58 ] Jullien H, Valot H, Polymer, 1985, 26, 506- 510.
[59 ] Lewis D A , Ward T C, Summers J S, First Australian Symposiumon Microwave Power Applications, Wollongong, 1989.
[60 ] Chen S T , Chiou S H, Wang K T , Int. J. Peptide Protein Res. , 1987, 30, 572- 576.
[61 ] Chiou S H, Wang K T , J. Chromatogr. Biomedical Applications, 1989, 491, 424- 431.
[62 ] Chen S T , Tseng P H, Yu H M et al. , J. Chinese Chem. Soc. , 1997, 44, 169- 182.
[63 ] Baghurst D R, Cooper S R, Greene D L et al. , Polyhedron, 1990, 9, 893- 895.
[64 ] Michael D, Mingos P, J. Chem. Soc. , Chem. Commun. , 1996, 899- 900.
[65 ] Hwang D R, Moerlein S M , Lang L et al. , J. Chem. Soc. , Chem. Commun. , 1987, 1799- 1801.
[66 ] Chen C G, Hong P J , Dai S H et al. , J. Chem. Soc. , Faraday Trans. , 1995, 91, 1179- 1180.
[67 ] Ioffe M S, Pollington S D, Wan J K S, J. Cat. , 1995, 151,349- 355.
[68 ] Tse M Y, Depew M C, Res. Chem. Inter. , 1990, 13, 221.

[1] 鄢剑锋, 徐进栋, 张瑞影, 周品, 袁耀锋, 李远明. 纳米碳分子——合成化学的魅力[J]. 化学进展, 2023, 35(5): 699-708.
[2] 王娜娜, 王官武. 机械研磨条件下凝聚态有机合成探究[J]. 化学进展, 2020, 32(8): 1076-1085.
[3] 缪谦, 杨代月. 从含有八元环的稠环芳烃到具有负曲率的碳纳米结构:进展与展望[J]. 化学进展, 2020, 32(11): 1835-1845.
[4] 付如刚, 李政, 高磊. 直接以碳化钙为炔源合成有机化合物[J]. 化学进展, 2019, 31(9): 1303-1313.
[5] 邹怀波, 汪华华, 梅光泉, 刘海洋, 张启光. 铁咔咯配合物在有机合成中的催化应用[J]. 化学进展, 2015, 27(6): 666-674.
[6] 徐艺凇, 张凤香, 厉嘉云, 白赢, 肖文军, 彭家建. 聚乙二醇功能化离子液体的制备及其在有机反应中的应用[J]. 化学进展, 2015, 27(10): 1400-1412.
[7] 沈海民, 武宏科, 史鸿鑫, 纪红兵, 余武斌. 非均相环糊精在水相有机合成反应中的应用[J]. 化学进展, 2015, 27(1): 70-78.
[8] 王爱玲, 郑学良, 赵壮志, 李长平, 郑学仿. 深共融溶剂在有机合成中的应用[J]. 化学进展, 2014, 26(05): 784-795.
[9] 徐立宁, 张军涛, 陶成, 曹小平. 烯氯化合物及其合成进展[J]. 化学进展, 2013, 25(11): 1876-1887.
[10] 侯晨, 朱浩, 李亦婧, 李彦锋*. 固定化脯氨酸及其衍生物用于催化不对称有机合成[J]. 化学进展, 2012, (9): 1729-1741.
[11] 王志会*, 王晓. 氮杂吲哚合成[J]. 化学进展, 2012, (10): 1974-1982.
[12] 沈金海, 程国林, 崔秀灵*. 基于钯催化C-H键活化的多米诺反应[J]. 化学进展, 2012, 24(07): 1324-1336.
[13] 包春燕*, 贾慧娟, 刘涛, 汪奕, 彭伟, 朱麟勇. 双分子层膜人工离子通道的合成[J]. 化学进展, 2012, 24(07): 1337-1345.
[14] 刘艳红, 周林成, 惠新平, 赵光辉, 李彦锋. 超顺磁性纳米催化剂在有机合成中的应用[J]. 化学进展, 2012, 24(0203): 327-337.
[15] 刘利 王东. “水上” (“on water”) 有机反应*[J]. 化学进展, 2010, 22(07): 1233-1241.
阅读次数
全文


摘要

微波促进有机化学反应研究进展